Linked Data
MyVariant Identifiers:
chr2:g.189910556A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189045830A>C , CM000664.2:g.189045830A>C | GRCh38 |
| NC_000002.11:g.189910556A>C , CM000664.1:g.189910556A>C | GRCh37 |
| NC_000002.10:g.189618801A>C | NCBI36 |
| NG_011799.1:g.139050T>G | |
| NG_011799.2:g.139050T>G | |
| NG_011799.3:g.184472T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.3279T>G MANE Select | ENSP00000364000.3:p.Ala1093= | |
| ENST00000374866.7:c.3279T>G | ENSP00000364000.3:p.Ala1093= | |
| ENST00000618828.1:c.2118T>G | ENSP00000482184.1:p.Ala706= | |
| NM_000393.3:c.3279T>G | NP_000384.2:p.Ala1093= | |
| XM_011510573.1:c.3141T>G | XP_011508875.1:p.Ala1047= | |
| NM_000393.4:c.3279T>G | NP_000384.2:p.Ala1093= | |
| XM_011510573.3:c.3141T>G | XP_011508875.1:p.Ala1047= | |
| NM_000393.5:c.3279T>G MANE Select | NP_000384.2:p.Ala1093= |